新型4-喹诺酮类衍生物氟罗沙星RO 23-6240的体外活性比较。

K Machka, I Braveny
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引用次数: 4

摘要

比较了RO 23-6240与诺氟沙星、氧氟沙星、环丙沙星等4种抗菌药物对345株近期临床分离菌株的体外抑菌活性。RO 23-6240对肠杆菌科和反硝化不动杆菌的mic≤0.5 mg/l。在相同浓度的化合物下,90%的葡萄球菌被抑制。RO 23-6240对粪肠球菌和铜绿假单胞菌活性较低,MIC90值分别为4.0 mg/l和8.0 mg/l。对哌拉西林、头孢噻肟和妥布霉素耐药的肠杆菌科和葡萄球菌对该化合物敏感。总的来说,RO 23-6240的活性与诺氟沙星和氧氟沙星相当,但低于环丙沙星。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative in vitro activity of RO 23-6240 (fleroxacin), a new 4-quinolone derivative.

The in vitro activity of RO 23-6240 was compared with that of norfloxacin, ofloxacin and ciprofloxacin as well as four other antimicrobial agents against 345 recent clinical isolates. The MICs of RO 23-6240 against Enterobacteriaceae and Acinetobacter anitratum was less than or equal to 0.5 mg/l. At the same concentration of the compound 90% of staphylococci were inhibited. Against Enterococcus faecalis and Pseudomonas aeruginosa RO 23-6240 proved less active, having MIC90 values of 4.0 mg/l and 8.0 mg/l, respectively. Enterobacteriaceae and staphylococci strains that were resistant to piperacillin, cefotaxime or tobramycin were susceptible to the compound. In general the activity of RO 23-6240 was comparable to those of norfloxacin and ofloxacin, but less than that of ciprofloxacin.

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